NDC 67296-2170
Nifedipine 30 mg tablet, extended release
On the label: RedPharm Drug. Inc.. It's repackaged: RedPharm Drug. Inc. rebottles it from Aurobindo Pharma Limited's NDC 59651-295.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Apl Healthcare Limited | Tirupati, India | Makes it and tests it | Problems found, fixed voluntarilyDec 17, 2025 · 5 inspections |
Repackaging site
- RedPharm Drug, Eden Prairie, MN, United States · repackages it
Product details
- Generic drug
- Nifedipine: every company that makes it
- Form
- tablet, extended release, oral
- Strength
- 30 mg
- Approval
- ANDA ANDA213361
- On the market since
- Jul 19, 2021
- Package NDCs
67296-2170-1- Official label
- DailyMed (National Library of Medicine), updated Dec 2, 2025
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